| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1420707-1421036 | Common:1; Rare:129 | ||||
| chr16:1493247-1493621 | Common:4; Rare:112 | ||||
| chr16:1706046-1706422 | Common:5; Rare:117 | ||||
| chr16:1771499-1771892 | Common:4; Rare:155 | ||||
| chr16:1782508-1783015 | Common:4; Rare:168 | ||||
| chr16:1943152-1943499 | Common:1; Rare:108 | ||||
| chr16:1959458-1959660 | Common:3; Rare:91 | ||||
| chr16:1964295-1964600 | Common:4; Rare:129 | ||||
| chr16:1964823-1965016 | Common:6; Rare:80 | ||||
| chr16:1971904-1972123 | Common:1; Rare:65 | ||||
| chr16:1984296-1984354 | Rare:19 | ||||
| chr16:2047727-2048050 | Rare:161; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2155468-2155828 | Common:2; Rare:102 | ||||
| chr16:2205683-2205932 | Common:5; Rare:116 | ||||
| chr16:2268066-2268520 | Common:5; Rare:159 |